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Current insights in ultra-rare adenylosuccinate synthetase 1 myopathy - meeting report on the First Clinical and Scientific Conference. 3 June 2024, National Centre for Advancing Translational Science, Rockville, Maryland, the United States of America

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dc.contributor.author박형준-
dc.date.accessioned2025-02-03T09:23:42Z-
dc.date.available2025-02-03T09:23:42Z-
dc.date.issued2024-11-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/202427-
dc.description.abstractThe inaugural Clinical and Scientific Conference on Adenylosuccinate Synthetase 1 (ADSS1) myopathy was held on June 3, 2024, at the National Institutes of Health (NIH) National Center for Advancing Translational Sciences (NCATS) in Rockville, Maryland, USA. ADSS1 myopathy is an ultra-rare, inherited neuromuscular disease. Features of geographical patient clusters in South Korea, Japan, India and the United States of America were characterised and discussed. Pre-clinical animal and cell-based models were discussed, providing unique insight into disease pathogenesis. The biochemical pathogenesis was discussed, and potential therapeutic targets identified. Potential clinical and pre-clinical biomarkers were discussed. An ADSS1 myopathy consortium was established and a roadmap for therapeutic development created.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherBioMed Central-
dc.relation.isPartOfORPHANET JOURNAL OF RARE DISEASES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleCurrent insights in ultra-rare adenylosuccinate synthetase 1 myopathy - meeting report on the First Clinical and Scientific Conference. 3 June 2024, National Centre for Advancing Translational Science, Rockville, Maryland, the United States of America-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Neurology (신경과학교실)-
dc.contributor.googleauthorEmma Rybalka-
dc.contributor.googleauthorHyung Jun Park-
dc.contributor.googleauthorAtchayaram Nalini-
dc.contributor.googleauthorDipti Baskar-
dc.contributor.googleauthorKiran Polavarapu-
dc.contributor.googleauthorHacer Durmus-
dc.contributor.googleauthorYang Xia-
dc.contributor.googleauthorLinlin Wan-
dc.contributor.googleauthorPerry B Shieh-
dc.contributor.googleauthorBehzad Moghadaszadeh-
dc.contributor.googleauthorAlan H Beggs-
dc.contributor.googleauthorDavid L Mack-
dc.contributor.googleauthorAlec S T Smith-
dc.contributor.googleauthorWendy Hanna-Rose-
dc.contributor.googleauthorHyder A Jinnah-
dc.contributor.googleauthorCara A Timpani-
dc.contributor.googleauthorMin Shen-
dc.contributor.googleauthorJaymin Upadhyay-
dc.contributor.googleauthorJeffrey J Brault-
dc.contributor.googleauthorMatthew D Hall-
dc.contributor.googleauthorNaveen Baweja-
dc.contributor.googleauthorPriyanka Kakkar-
dc.identifier.doi10.1186/s13023-024-03429-x-
dc.contributor.localIdA01758-
dc.relation.journalcodeJ03433-
dc.identifier.eissn1750-1172-
dc.identifier.pmid39593137-
dc.subject.keywordADSS1 myopathy-
dc.subject.keywordAdenylosuccinate synthetase 1 myopathy-
dc.subject.keywordBiomarkers-
dc.subject.keywordCardiac muscle-
dc.subject.keywordClinical presentation-
dc.subject.keywordConsortium-
dc.subject.keywordGuidelines-
dc.subject.keywordInborn error of metabolism-
dc.subject.keywordPre-clinical models-
dc.subject.keywordPurine disorder-
dc.subject.keywordSkeletal muscle-
dc.subject.keywordTherapeutics-
dc.subject.keywordUltra-rare neuromuscular disease-
dc.contributor.alternativeNamePark, Hyung Jun-
dc.contributor.affiliatedAuthor박형준-
dc.citation.volume19-
dc.citation.startPage438-
dc.identifier.bibliographicCitationORPHANET JOURNAL OF RARE DISEASES, Vol.19 : 438, 2024-11-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Neurology (신경과학교실) > 1. Journal Papers

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